University of California - San Francisco Campus and Health
Clinical Research Coordinator - Gynecologic Oncology Program
University of California - San Francisco Campus and Health, San Francisco, California, United States, 94199
Clinical Research Coordinator - Gynecologic Oncology Program
HDF Comprehensive Cancer Ctr Full Time 86215BR Overview
The Gynecologic Oncology program has a multi-disciplinary team that works closely with patients, providing the resources and close cooperation of many specialists with deep expertise in diagnosing and treating cancer. Our physician-scientists are also researching and developing new and effective treatments for Gynecologic cancer, including clinical trials. The Gynecologic Oncology program is seeking a Clinical Research Coordinator with an interest in women's health to have oversight over multiple clinical research projects and support our growing program. The Clinical Research Coordinator (CRC) will independently, or with general direction, execute, manage, and coordinate clinical research protocols, as directed by the Clinical Research Manager, Principal Investigator (PI), and/or the Associate Director of Clinical Research Programs for the Early Phase program. The CRC will coordinate the administrative, data, and patient scheduling operations of several concurrent clinical research studies under the guidelines of research protocols and regulatory policies. The CRC will assist in the care of early and late-stage Gynecologic cancer patients while they participate in phase1b - phase 3 clinical trials. Responsibilities
Support the management and coordination of single or multiple clinical research studies. Manage and update databases to ensure data integrity. Act as intermediary between sponsors, research staff, and UCSF departments; ensure compliance with regulatory policies. Maintain regulatory documents in partnership with the Regulatory department. Report study progress to investigators. Participate in internal and external audits or reviews of study protocols. Perform other duties as assigned. The final salary and offer components are subject to additional approvals based on UC policy. Your placement within the salary range is dependent on factors including work experience and internal equity within this position classification at UCSF; for represented positions, placement follows the collective bargaining agreement. The salary range for this position is $34.32 - $55.19 (Hourly Rate). To learn more about benefits of working at UCSF, including total compensation, please visit: https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html Department Description
The UCSF Helen Diller Family Comprehensive Cancer Center (HDFCCC) holds the designation of "comprehensive" from the National Cancer Institute (NCI). We combine basic science, clinical research, epidemiology, cancer control and patient care throughout UCSF. Required Qualifications
HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; or equivalent experience/training. Attention to detail; strong interpersonal skills; excellent verbal and written communication skills to coordinate with subjects, team members, other departments and outside institutions; ability to multi-task in a fast-paced environment while working with a diverse subject population. Ability to work well independently, complete projects in a timely manner, and prioritize multiple projects to ensure completion of essential tasks by deadlines. Preferred Qualifications
Prior analytical and writing skills in a science/research environment. Knowledge of clinical research in oncology; experience managing oncology clinical trials. Membership in a clinical research professional society; demonstrated knowledge of research in biological sciences. Experience with electronic medical records and software such as Microsoft Office; familiarity with OnCore. Ability to sit and work at a computer for several hours per day; potential campus travel via UCSF shuttle; able to stand for extended periods. Experience in clinical research or related training, with ability to learn specimen processing in a laboratory setting. Understanding of federal, state, and local research regulations and guidelines; ability to apply policies and respond to requests in a team environment. Knowledge of medical terminology and ability to apply it to data interpretation and processing. Ability to work with oncology patients and across multiple programs reporting to 2-3 supervisors. Familiarity with CHR online iMEDris system for protocol submission, renewal, and modification; understanding of patient participation considerations. Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals. Knowledge of UCSF policies for reimbursement, research guidelines, confidentiality and HIPAA, patient safety and confidentiality; experience with data management and statistical software (e.g., Access, Stata, SPSS). Experience applying Good Clinical Practice, HIPAA, and CHR regulations, and related safety and environmental health trainings. About UCSF
The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and excellence in patient care. It is the only campus in the 10-campus UC system dedicated exclusively to the health sciences, and hosts many renowned researchers and clinicians. Pride Values
UCSF values professionalism, respect, integrity, diversity and excellence (PRIDE). UCSF is committed to equity and building a diverse, welcoming community. Additional information about UCSF diversity is available at diversity.ucsf.edu. Join us to find a rewarding career contributing to improving healthcare worldwide. Equal Employment Opportunity
The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law. Organization
Campus Job Code and Payroll Title
009335 CLIN RSCH CRD Job Category
Research and Scientific Bargaining Unit
University Professional Technical Employees - Research Support Professionals Unit (UPTE-RX) Employee Class
Career Percentage
100% Location
San Francisco, CA Campus
Mission Bay (SF) Work Style
Flexible Shift
Days Shift Length
8 Hours Additional Shift Details
Monday - Friday
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HDF Comprehensive Cancer Ctr Full Time 86215BR Overview
The Gynecologic Oncology program has a multi-disciplinary team that works closely with patients, providing the resources and close cooperation of many specialists with deep expertise in diagnosing and treating cancer. Our physician-scientists are also researching and developing new and effective treatments for Gynecologic cancer, including clinical trials. The Gynecologic Oncology program is seeking a Clinical Research Coordinator with an interest in women's health to have oversight over multiple clinical research projects and support our growing program. The Clinical Research Coordinator (CRC) will independently, or with general direction, execute, manage, and coordinate clinical research protocols, as directed by the Clinical Research Manager, Principal Investigator (PI), and/or the Associate Director of Clinical Research Programs for the Early Phase program. The CRC will coordinate the administrative, data, and patient scheduling operations of several concurrent clinical research studies under the guidelines of research protocols and regulatory policies. The CRC will assist in the care of early and late-stage Gynecologic cancer patients while they participate in phase1b - phase 3 clinical trials. Responsibilities
Support the management and coordination of single or multiple clinical research studies. Manage and update databases to ensure data integrity. Act as intermediary between sponsors, research staff, and UCSF departments; ensure compliance with regulatory policies. Maintain regulatory documents in partnership with the Regulatory department. Report study progress to investigators. Participate in internal and external audits or reviews of study protocols. Perform other duties as assigned. The final salary and offer components are subject to additional approvals based on UC policy. Your placement within the salary range is dependent on factors including work experience and internal equity within this position classification at UCSF; for represented positions, placement follows the collective bargaining agreement. The salary range for this position is $34.32 - $55.19 (Hourly Rate). To learn more about benefits of working at UCSF, including total compensation, please visit: https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html Department Description
The UCSF Helen Diller Family Comprehensive Cancer Center (HDFCCC) holds the designation of "comprehensive" from the National Cancer Institute (NCI). We combine basic science, clinical research, epidemiology, cancer control and patient care throughout UCSF. Required Qualifications
HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; or equivalent experience/training. Attention to detail; strong interpersonal skills; excellent verbal and written communication skills to coordinate with subjects, team members, other departments and outside institutions; ability to multi-task in a fast-paced environment while working with a diverse subject population. Ability to work well independently, complete projects in a timely manner, and prioritize multiple projects to ensure completion of essential tasks by deadlines. Preferred Qualifications
Prior analytical and writing skills in a science/research environment. Knowledge of clinical research in oncology; experience managing oncology clinical trials. Membership in a clinical research professional society; demonstrated knowledge of research in biological sciences. Experience with electronic medical records and software such as Microsoft Office; familiarity with OnCore. Ability to sit and work at a computer for several hours per day; potential campus travel via UCSF shuttle; able to stand for extended periods. Experience in clinical research or related training, with ability to learn specimen processing in a laboratory setting. Understanding of federal, state, and local research regulations and guidelines; ability to apply policies and respond to requests in a team environment. Knowledge of medical terminology and ability to apply it to data interpretation and processing. Ability to work with oncology patients and across multiple programs reporting to 2-3 supervisors. Familiarity with CHR online iMEDris system for protocol submission, renewal, and modification; understanding of patient participation considerations. Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals. Knowledge of UCSF policies for reimbursement, research guidelines, confidentiality and HIPAA, patient safety and confidentiality; experience with data management and statistical software (e.g., Access, Stata, SPSS). Experience applying Good Clinical Practice, HIPAA, and CHR regulations, and related safety and environmental health trainings. About UCSF
The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and excellence in patient care. It is the only campus in the 10-campus UC system dedicated exclusively to the health sciences, and hosts many renowned researchers and clinicians. Pride Values
UCSF values professionalism, respect, integrity, diversity and excellence (PRIDE). UCSF is committed to equity and building a diverse, welcoming community. Additional information about UCSF diversity is available at diversity.ucsf.edu. Join us to find a rewarding career contributing to improving healthcare worldwide. Equal Employment Opportunity
The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law. Organization
Campus Job Code and Payroll Title
009335 CLIN RSCH CRD Job Category
Research and Scientific Bargaining Unit
University Professional Technical Employees - Research Support Professionals Unit (UPTE-RX) Employee Class
Career Percentage
100% Location
San Francisco, CA Campus
Mission Bay (SF) Work Style
Flexible Shift
Days Shift Length
8 Hours Additional Shift Details
Monday - Friday
#J-18808-Ljbffr